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Chemical structure of CAS 622-78-6

Benzyl Isothiocyanate

In Stock•Starting at $6 for 1 g•Purity ≥ 98%
CAS No.622-78-6
MDL No.MFCD00004819
MFC8H7NS
MW149.21
InChI KeyMDKCFLQDBWCQCV-UHFFFAOYSA-N
CUSTOM SYNTHESISPRECLINICAL SUPPORT

Pricing & Availability

Pack SizePurityPriceAvailabilityAction
1 g98%$6In Stock
5 g98%$10In Stock
10 g98%$14In Stock
25 g98%$25In Stock
4*25 g98%$97In Stock
Custom synthesis and bulk supply options are available upon request.

Product Information

Benzyl isothiocyanate is an isothiocyanate belonging to the benzene class, and functions as an antibacterial drug.

CAS No.622-78-6
Product NameBenzyl Isothiocyanate
IrritantIrritant
Signal Word:Warning
HCode:H319-H335
PCode:P261-P264+P265-P271-P280-P304+P340-P305+P351+P338-P319-P337+P317-P403+P233-P405-P501

Related Articles

Studies related to this compound and its mechanism of action

Involvement of the mitochondrial death pathway in chemopreventive benzyl isothiocyanate-induced apoptosis.

The Journal of biological chemistry • Vol. 277, Issue 10 • 2002
PMID: 11751909DOI: 10.1074/jbc.M109760200

Inhibition of benzo(a)pyrene-induced lung tumorigenesis in A/J mice by dietary N-acetylcysteine conjugates of benzyl and phenethyl isothiocyanates during the postinitiation phase is associated with activation of mitogen-activated protein kinases and p53 activity and induction of apoptosis.

Cancer research • Vol. 62, Issue 1 • 2002
PMID: 11782348

Palladium(0)-catalyzed enantioselective O,S-rearrangement of racemic O-allylic thiocarbamates: a new entry to enantioenriched allylic sulfur compounds.

The Journal of organic chemistry • Vol. 67, Issue 4 • 2002
PMID: 11846656DOI: 10.1021/jo010668b

Effects of benzyl isothiocyanate on rat and human cytochromes P450: identification of metabolites formed by P450 2B1.

The Journal of pharmacology and experimental therapeutics • Vol. 296, Issue 1 • 2001
PMID: 11123381

Documentation

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